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A Low Incidence of Posttransplant Lymphoproliferative Disorder in 109 Lung Transplant Recipients

Authors :
Edward Y. Sako
C. L. Bryan
Jay I Peters
Antonio Anzueto
Luis F. Angel
Stephanie M Levine
Irawan Susanto
Source :
Chest. 116:1273-1277
Publication Year :
1999
Publisher :
Elsevier BV, 1999.

Abstract

Study objectives: The incidence of posttransplant lymphoproliferative disorder (PTLD) has been reported to range from 6.4 to 20% in lung transplant (LT) recipients. Postulated contributing factors include Epstein-Barr virus (EBV) infection and the use of immunosuppression, particularly muromonab-CD3 (OKT3)(Orthoclone OKT-3; Ortho Biotech; Raritan, NJ). We sought to examine these PTLD risk factors in 109 LT recipients at our institution who survived > 1 month. Design: Retrospective review of EBV serology of all LT recipients at our institution. Our standard transplant protocol includes OKT3 for induction and refractory rejection, as well as lifelong acyclovir for herpes prophylaxis. We do not perform EBV donor-recipient matching. Setting: A university-based LT center. Results: We found that 5 of 109 patients were serologically negative for EBV prior to lung transplantation, and all of these patients converted following lung transplantation. The mean time to conversion was 151 days (range, 11 to 365 days). One fatal case of PTLD was documented in an EBV seroconverter (one of five patients) 12 weeks status posttransplantation for lymphangioleiomyomatosis. One nonfatal extrathoracic PTLD was documented in a seropositive patient (1 of 104 patients) 33 months posttransplantation. Conclusions: We conclude the following: (1) PTLD in LT recipients may have a lower incidence (2 of 109 patients; 1.8%) than previously reported, despite an aggressive immunosuppressive regimen; and (2) the incidence of PTLD is higher in patients with primary EBV infection (20% vs 1%). (CHEST 1999; 116:1273‐1277)

Details

ISSN :
00123692
Volume :
116
Database :
OpenAIRE
Journal :
Chest
Accession number :
edsair.doi.dedup.....161f46ea08e0061cad78e002f2c8623a
Full Text :
https://doi.org/10.1378/chest.116.5.1273